T2 Plus
K-Number: K233806 · 2024-09-06
ApplicantOsstem Implant Co., Ltd.
Decision Date2024-09-06
Product CodeOAS
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
T2 Plus is a medical device manufactured by Osstem Implant Co., Ltd.. It received FDA 510(k) clearance on 2024-09-06 under approval number K233806. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the T2 Plus?
T2 Plus is a medical device that received FDA 510(k) clearance on 2024-09-06. It is manufactured by Osstem Implant Co., Ltd.. The 510(k) number is K233806.
When was T2 Plus approved by the FDA?
T2 Plus received FDA 510(k) clearance on 2024-09-06, under approval number K233806.
What company makes T2 Plus?
T2 Plus is manufactured by Osstem Implant Co., Ltd..
What is the FDA product code for T2 Plus?
The FDA product code for T2 Plus is OAS.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.